Variant report

Variant	rs2441885
Chromosome Location	chr8:105188914-105188915
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10102063	0.86[EUR][1000 genomes]
rs1060441	0.92[EUR][1000 genomes]
rs2441790	0.91[EUR][1000 genomes]
rs2441794	0.90[EUR][1000 genomes]
rs2441802	0.85[EUR][1000 genomes]
rs2441815	0.92[EUR][1000 genomes]
rs2441818	0.92[EUR][1000 genomes]
rs2441819	0.92[EUR][1000 genomes]
rs2441821	0.92[EUR][1000 genomes]
rs2441823	0.92[EUR][1000 genomes]
rs2441824	0.92[EUR][1000 genomes]
rs2441826	0.92[EUR][1000 genomes]
rs2441827	0.92[EUR][1000 genomes]
rs2441832	0.90[EUR][1000 genomes]
rs2441850	0.86[EUR][1000 genomes]
rs2441851	0.85[EUR][1000 genomes]
rs2441895	0.82[EUR][1000 genomes]
rs2441896	0.82[EUR][1000 genomes]
rs2441902	0.95[EUR][1000 genomes]
rs2441905	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2441907	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2441910	0.97[EUR][1000 genomes]
rs2511553	0.97[EUR][1000 genomes]
rs2511580	0.93[EUR][1000 genomes]
rs2511585	0.92[EUR][1000 genomes]
rs2511587	0.92[EUR][1000 genomes]
rs2511590	0.91[EUR][1000 genomes]
rs2511594	0.92[EUR][1000 genomes]
rs2511595	0.92[EUR][1000 genomes]
rs2511597	0.92[EUR][1000 genomes]
rs2511598	0.84[EUR][1000 genomes]
rs2511602	0.92[EUR][1000 genomes]
rs2511603	0.92[EUR][1000 genomes]
rs2511605	0.85[EUR][1000 genomes]
rs2511606	0.83[EUR][1000 genomes]
rs2511609	0.86[EUR][1000 genomes]
rs2511626	0.83[EUR][1000 genomes]
rs2511640	0.97[EUR][1000 genomes]
rs2511641	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2511643	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2511646	0.97[EUR][1000 genomes]
rs2511648	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2514631	0.84[EUR][1000 genomes]
rs2514632	0.83[EUR][1000 genomes]
rs2514640	0.82[EUR][1000 genomes]
rs2514645	0.82[EUR][1000 genomes]
rs2514652	0.90[EUR][1000 genomes]
rs2514659	0.89[EUR][1000 genomes]
rs2514672	0.86[EUR][1000 genomes]
rs3099574	0.97[EUR][1000 genomes]
rs750432	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031195	chr8:104601231-105194208	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
2	esv1847227	chr8:105025912-105251147	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv891251	chr8:105054446-105283340	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
4	nsv891252	chr8:105106882-105227985	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv831416	chr8:105137789-105296965	Flanking Active TSS Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:105188400-105211800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:105188600-105189600	Enhancers	HMEC	breast
3	chr8:105188600-105190800	Enhancers	NHEK	skin
4	chr8:105188800-105189400	Enhancers	GM12878-XiMat	blood
5	chr8:105188800-105190200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:105188800-105190400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:105188800-105192800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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